Volatile Oil Containing Plants as Phytopharmaceuticals to Treat Psoriasis: A Review
- Authors: Vyas P.1, Wagh S.1, Kalaskar M.1, Patil K.1, Sharma A.2, Kazmi I.3, Al-Abbasi F.4, Alzarea S.5, Afzal O.6, Altamimi A.6, Gupta G.7, Patil C.2
-
Affiliations:
- , R. C. Patel Institute of Pharmaceutical Education and Research
- Department of Pharmacognosy, School of Pharmaceutical Sciences, Delhi Pharmaceutical Sciences & Research University
- Department of Biochemistry, Faculty of Scienceof Biochemistry, Faculty of Science, King Abdulaziz University
- Department of Biochemistry, Faculty of Science, King Abdulaziz University
- Department of Pharmacology, College of Pharmacy,, Jouf University
- Department of Pharmaceutical Chemistry, College of Pharmacy,, Prince Sattam Bin Abdulaziz University
- Department of Pharmacology, School of Pharmacy,, Suresh Gyan Vihar University
- Issue: Vol 25, No 3 (2024)
- Pages: 313-339
- Section: Biotechnology
- URL: https://vietnamjournal.ru/1389-2010/article/view/644775
- DOI: https://doi.org/10.2174/1389201024666230607140404
- ID: 644775
Cite item
Full Text
Abstract
Introduction:Psoriasis is a chronic skin condition caused by an autoimmune response that accelerates the life cycle of skin cells, resulting in the characteristic symptoms of scaling, inflammation, and itching.
Methods:Palliative treatment options for psoriasis often prioritize the use of volatile oils. These oils contain monoterpenes, sesquiterpenes, and phenylpropanoids that are intricately linked to the molecular cascades involved in the pathogenesis and symptoms of psoriasis. To evaluate the antipsoriatic efficacy of volatile oils and their components, we conducted a systematic review of scientific studies. Our literature search encompassed various online databases, including PubMed, BIREME, SCIELO, Open Grey, Scopus, and ScienceDirect. The selected studies included experimental in vitro/in vivo assessments as well as clinical studies that examined the potential of volatile oils and their extracts as antipsoriatic agents. We excluded conference proceedings, case reports, editorials, and abstracts. Ultimately, we identified and evaluated a total of 12 studies for inclusion in our analysis.
Results:The data collected, compiled, and analyzed strongly support the interaction between volatile oils and their constituents with the key molecular pathways involved in the pathogenesis of psoriasis and the development of its symptoms. Volatile oils play a significant role in the palliative treatment of psoriasis, while their chemical constituents have the potential to reduce the symptoms and recurrence of this condition.
Conclusion:The current review highlights that the constituents found in volatile oils offer distinct chemical frameworks that can be regarded as promising starting points for the exploration and development of innovative antipsoriatic agents.
Keywords
About the authors
Priyanka Vyas
, R. C. Patel Institute of Pharmaceutical Education and Research
Email: info@benthamscience.net
Shivani Wagh
, R. C. Patel Institute of Pharmaceutical Education and Research
Email: info@benthamscience.net
Mohan Kalaskar
, R. C. Patel Institute of Pharmaceutical Education and Research
Email: info@benthamscience.net
Kalpesh Patil
, R. C. Patel Institute of Pharmaceutical Education and Research
Email: info@benthamscience.net
Ajay Sharma
Department of Pharmacognosy, School of Pharmaceutical Sciences, Delhi Pharmaceutical Sciences & Research University
Author for correspondence.
Email: info@benthamscience.net
Imran Kazmi
Department of Biochemistry, Faculty of Scienceof Biochemistry, Faculty of Science, King Abdulaziz University
Email: info@benthamscience.net
Fahad Al-Abbasi
Department of Biochemistry, Faculty of Science, King Abdulaziz University
Email: info@benthamscience.net
Sami Alzarea
Department of Pharmacology, College of Pharmacy,, Jouf University
Email: info@benthamscience.net
Obaid Afzal
Department of Pharmaceutical Chemistry, College of Pharmacy,, Prince Sattam Bin Abdulaziz University
Email: info@benthamscience.net
Abdulmalik Altamimi
Department of Pharmaceutical Chemistry, College of Pharmacy,, Prince Sattam Bin Abdulaziz University
Email: info@benthamscience.net
Gaurav Gupta
Department of Pharmacology, School of Pharmacy,, Suresh Gyan Vihar University
Email: info@benthamscience.net
Chandragouda Patil
Department of Pharmacognosy, School of Pharmaceutical Sciences, Delhi Pharmaceutical Sciences & Research University
Author for correspondence.
Email: info@benthamscience.net
References
- Ayala-Fontánez, N.; Soler, D.C.; McCormick, T.S. Current knowledge on psoriasis and autoimmune diseases. Psoriasis, 2016, 6, 7-32. PMID: 29387591
- Fu, Y.; Lee, C.H.; Chi, C.C. Association of psoriasis with inflammatory bowel disease: A systematic review and meta-analysis. JAMA Dermatol., 2018, 154(12), 1417-1423. doi: 10.1001/jamadermatol.2018.3631 PMID: 30422277
- García-Sánchez, L.; Montiel-Jarquín, A.J.; Vázquez-Cruz, E.; May-Salazar, A.; Gutiérrez-Gabriel, I.; Loría-Castellanoso, J. Quality of life in patients with psoriasis. Gac. Med. Mex., 2017, 153(2), 185-189. PMID: 28474705
- Lai, C.Y.; Su, Y.W.; Lin, K.I.; Hsu, L.C. Natural modulators of endosomal toll-like receptor-mediated psoriatic skin inflammation. J. Immunol. Res., 2017, 2017, 7807313.
- Boutet, M.A.; Nerviani, A.; Gallo Afflitto, G.; Pitzalis, C. Role of the IL-23/IL-17 Axis in Psoriasis and Psoriatic Arthritis: The clinical importance of its divergence in skin and joints. Int. J. Mol. Sci., 2018, 19(2), 530. doi: 10.3390/ijms19020530 PMID: 29425183
- Langrish, C.L.; Chen, Y.; Blumenschein, W.M.; Mattson, J.; Basham, B.; Sedgwick, J.D.; McClanahan, T.; Kastelein, R.A.; Cua, D.J. IL-23 drives a pathogenic T cell population that induces autoimmune inflammation. J. Exp. Med., 2005, 201(2), 233-240. doi: 10.1084/jem.20041257 PMID: 15657292
- Park, H.; Li, Z.; Yang, X.O.; Chang, S.H.; Nurieva, R.; Wang, Y.H.; Wang, Y.; Hood, L.; Zhu, Z.; Tian, Q.; Dong, C. A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17. Nat. Immunol., 2005, 6(11), 1133-1141. doi: 10.1038/ni1261 PMID: 16200068
- Georgescu, S.R.; Tampa, M.; Caruntu, C.; Sarbu, M.I. Advances in understanding the immunological pathways in psoriasis. Int. J. Mol. Sci., 2019, 20(3), 739.
- Lipton, J.O.; Sahin, M. The neurology of mTOR. Neuron, 2014, 84(2), 275-291. doi: 10.1016/j.neuron.2014.09.034 PMID: 25374355
- Bürger, C.; Shirsath, N.; Lang, V.; Diehl, S.; Kaufmann, R.; Weigert, A.; Han, Y.Y.; Ringel, C.; Wolf, P. Blocking mTOR Signalling with Rapamycin Ameliorates Imiquimod-induced Psoriasis in Mice. Acta Derm. Venereol., 2017, 97(9), 1087-1094. doi: 10.2340/00015555-2724 PMID: 28597024
- Chamcheu, J.C.; Chaves-Rodriquez, M.I.; Adhami, V.M.; Siddiqui, I.A.; Wood, G.S.; Longley, B.J.; Mukhtar, H. Upregulation of PI3K/AKT/mTOR, FABP5 and PPARβ/δ in Human Psoriasis and Imiquimod-induced Murine Psoriasiform Dermatitis Model. Acta Derm. Venereol., 2016, 96(6), 854-856. PMID: 26833029
- Tang, L.; Yang, X.; Liang, Y.; Xie, H.; Dai, Z.; Zheng, G. Transcription factor retinoid-related orphan receptor γt: A promising target for the treatment of psoriasis. Front. Immunol., 2018, 9, 1210. doi: 10.3389/fimmu.2018.01210 PMID: 29899748
- Aaronson, D.S.; Horvath, C.M. A road map for those who dont know JAK-STAT. Science, 2002, 296(5573), 1653-1655. doi: 10.1126/science.1071545 PMID: 12040185
- Damsky, W.; King, B.A. JAK inhibitors in dermatology: The promise of a new drug class. J. Am. Acad. Dermatol., 2017, 76(4), 736-744. doi: 10.1016/j.jaad.2016.12.005 PMID: 28139263
- Welsch, K.; Holstein, J.; Laurence, A.; Ghoreschi, K. Targeting JAK/STAT signalling in inflammatory skin diseases with small molecule inhibitors. Eur. J. Immunol., 2017, 47(7), 1096-1107.
- Hsu, L.; Armstrong, A.W. JAK inhibitors: Treatment efficacy and safety profile in patients with psoriasis. J. Immunol. Res., 2014, 2014, 283617. doi: 10.1155/2014/283617 PMID: 24883332
- Johansen, C.; Rittig, A.H.; Mose, M.; Bertelsen, T.; Weimar, I.; Nielsen, J.; Andersen, T.; Rasmussen, T.K.; Deleuran, B.; Iversen, L. STAT2 is involved in the pathogenesis of psoriasis by promoting CXCL11 and CCL5 production by keratinocytes. PLoS One, 2017, 12(5), e0176994. doi: 10.1371/journal.pone.0176994 PMID: 28472186
- Tsuji, F.; Aono, H. Role of transient receptor potential vanilloid 1 in inflammation and autoimmune diseases. Pharmaceuticals (Basel), 2012, 5(8), 837-852. doi: 10.3390/ph5080837 PMID: 24280677
- Lee, Y.M.; Kang, S.M.; Chung, J.H. The role of TRPV1 channel in aged human skin. J. Dermatol. Sci., 2012, 65(2), 81-85. doi: 10.1016/j.jdermsci.2011.11.003 PMID: 22154816
- Zhou, Y.; Follansbee, T.; Wu, X.; Han, D.; Yu, S.; Domocos, D.T.; Shi, Z.; Carstens, M.; Carstens, E.; Hwang, S.T. TRPV1 mediates inflammation and hyperplasia in imiquimod (IMQ)-induced psoriasiform dermatitis (PsD) in mice. J. Dermatol. Sci., 2018, 92(3), 264-271. doi: 10.1016/j.jdermsci.2018.11.009 PMID: 30527377
- Romac, J.; Liddle, R.A. Transient Receptor Potential Vanilloid 1 (TRPV1), Pancreapedia; The Exocrine Pancreas Knowledge Base, 2012.
- Malakou, L.S.; Gargalionis, A.N.; Piperi, C.; Papadavid, E.; Papavassiliou, A.G.; Basdra, E.K. Molecular mechanisms of mechanotransduction in psoriasis. Ann. Transl. Med., 2018, 6(12), 245. doi: 10.21037/atm.2018.04.09 PMID: 30069447
- Woo, Y.R.; Cho, D.H.; Park, H.J. Molecular mechanisms and management of a cutaneous inflammatory disorder. Psoriasis. Int. J. Mol. Sci., 2017, 18(12), 2684. doi: 10.3390/ijms18122684 PMID: 29232931
- Rácz, E.; Prens, E.P. Molecular pathophysiology of psoriasis and molecular targets of antipsoriatic therapy. Expert Rev. Mol. Med., 2009, 11, e38. doi: 10.1017/S146239940900129X PMID: 20003607
- Rigano, D.; Sirignano, C.; Taglialatela-Scafati, O. The potential of natural products for targeting PPARα. Acta Pharm. Sin. B, 2017, 7(4), 427-438. doi: 10.1016/j.apsb.2017.05.005 PMID: 28752027
- Sertznig, P.; Reichrath, J. Peroxisome proliferator-activated receptors (PPARs) in dermatology: Challenge and promise. Dermatoendocrinol, 2011, 3(3), 130-135. doi: 10.4161/derm.15025 PMID: 22110772
- Mavropoulos, A.; Rigopoulou, E.I.; Liaskos, C.; Bogdanos, D.P.; Sakkas, L.I. The role of p38 MAPK in the aetiopathogenesis of psoriasis and psoriatic arthritis. Clin. Dev. Immunol., 2013, 2013, 569751. doi: 10.1155/2013/569751 PMID: 24151518
- Tse, W.P.; Che, C.T.; Liu, K.; Lin, Z.X. Evaluation of the antiproliferative properties of selected psoriasis-treating Chinese medicines on cultured HaCaT cells. J. Ethnopharmacol., 2006, 108(1), 133-141. doi: 10.1016/j.jep.2006.04.023 PMID: 16730935
- Lin, Z.X.; Jiao, B.W.; Che, C.T.; Zuo, Z.; Mok, C.F.; Zhao, M.; Ho, W.K.K.; Tse, W.P.; Lam, K.Y.; Fan, R.Q.; Yang, Z.J.; Cheng, C.H.K. Ethyl acetate fraction of the root of Rubia cordifolia L. inhibits keratinocyte proliferation in vitro and promotes keratinocyte differentiation in vivo: Potential application for psoriasis treatment. Phytother. Res., 2010, 24(7), 1056-1064. doi: 10.1002/ptr.3079 PMID: 19960426
- Togni, S.; Maramaldi, G.; Di Pierro, F.; Biondi, M. A cosmeceutical formulation based on boswellic acids for the treatment of erythematous eczema and psoriasis. Clin. Cosmet. Investig. Dermatol., 2014, 7, 321-327. PMID: 25419153
- Gramosa, N.; Silveira, E.; Cavalcanti, B.; Ferreira, J.d.O.; Almeida, F.; Rao, V.; Costa-Lotufo, L.; de Moraes, M.; Pessoa, C. Chemistry and pharmacology of Copaifera langsdorffii Desf.: an overview. Drug plants I, 2010, 235-260.
- Li, K.; Yang, W.; Li, Z.; Jia, W.; Li, J.; Zhang, P.; Xiao, T. Bitter apricot essential oil induces apoptosis of human HaCaT keratinocytes. Int. Immunopharmacol., 2016, 34, 189-198. doi: 10.1016/j.intimp.2016.02.019 PMID: 26971222
- Kumar, S.; Singh, K.K.; Rao, R. Enhanced anti-psoriatic efficacy and regulation of oxidative stress of a novel topical babchi oil (Psoralea corylifolia) cyclodextrin-based nanogel in a mouse tail model. J. Microencapsul., 2019, 36(2), 140-155. doi: 10.1080/02652048.2019.1612475 PMID: 31030587
- Lee, Y.J.; Hong, I.K.; Kim, H.; Heo, S.I.; Kwon, D.J.; Ahn, W.G.; Kim, Y.H.; Seo, E.J.; Han, S.I.; Cho, H.J.; Kim, S.Y.; Yang, H. The Amelioration Effect of the Ethanolic Extract of Cnidium officinale in Mice with Imiquimod-induced Psoriasis-like Skin Lesion. Nat. Prod. Sci., 2018, 24(1), 21-27. doi: 10.20307/nps.2018.24.1.21
- Pazyar, N.; Yaghoobi, R. Tea tree oil as a novel antipsoriasis weapon. Skin Pharmacol. Physiol., 2012, 25(3), 162-163. doi: 10.1159/000337936 PMID: 22473218
- Enshaieh, S.; Jooya, A.; Siadat, A.H.; Iraji, F. The efficacy of 5% topical tea tree oil gel in mild to moderate acne vulgaris: a randomized, double-blind placebo-controlled study. Indian J. Dermatol. Venereol. Leprol., 2007, 73(1), 22-25. doi: 10.4103/0378-6323.30646 PMID: 17314442
- Okasha, E.F.; Bayomy, N.A.; Abdelaziz, E.Z. Effect of topical application of black seed oil on imiquimod-induced psoriasis-like lesions in the thin skin of adult male albino rats. Anat. Rec. (Hoboken), 2018, 301(1), 166-174. doi: 10.1002/ar.23690 PMID: 28926201
- Sharma, M.; Levenson, C.; Clements, I.; Castella, P.; Gebauer, K.; Cox, M.E. East Indian sandalwood oil (EISO) alleviates inflammatory and proliferative pathologies of psoriasis. Front. Pharmacol., 2017, 8, 125. doi: 10.3389/fphar.2017.00125 PMID: 28360856
- Langley, R.G.B.; Feldman, S.R.; Nyirady, J.; van de Kerkhof, P.; Papavassilis, C. The 5-point Investigators Global Assessment (IGA) Scale: A modified tool for evaluating plaque psoriasis severity in clinical trials. J. Dermatolog. Treat., 2015, 26(1), 23-31. doi: 10.3109/09546634.2013.865009 PMID: 24354461
- Muttalib, L.; Adham, A.; Ali, S.; Naqishbandi, A. Open-label uncontrolled pilot study on antipsoriatic activity of Rosa hemisphaerica. Zanco J. Med. Sci., 2017, 21(1), 1636-1644. doi: 10.15218/zjms.2017.014
- Jou, Y.J.; Hua, C.H.; Lin, C.S.; Wang, C.Y.; Wan, L.; Lin, Y.J.; Huang, S.H.; Lin, C.W. Anticancer activity of γ-bisabolene in human neu-roblastoma cells via induction of p53-mediated mitochondrial apoptosis. Molecules, 2016, 21(5), 601. doi: 10.3390/molecules21050601 PMID: 27164076
- Zhang, Y.; Wang, X.; Ma, L.; Dong, L.; Zhang, X.; Chen, J.; Fu, X. Anti-inflammatory, antinociceptive activity of an essential oil recipe consisting of the supercritical fluid CO2 extract of white pepper, long pepper, cinnamon, saffron and myrrh in vivo. J. Oleo Sci., 2014, 63(12), 1251-1260. doi: 10.5650/jos.ess14061 PMID: 25263165
- Leyva-López, N.; Nair, V.; Bang, W.Y.; Cisneros-Zevallos, L.; Heredia, J.B. Protective role of terpenes and polyphenols from three species of Oregano (Lippia graveolens, Lippia palmeri and Hedeoma patens) on the suppression of lipopolysaccharide-induced inflammation in RAW 264.7 macrophage cells. J. Ethnopharmacol., 2016, 187, 302-312. doi: 10.1016/j.jep.2016.04.051 PMID: 27131433
- Sitarek, P.; Rijo, P.; Garcia, C.; Skała, E.; Kalemba, D.; Białas, A.J.; Szemraj, J.; Pytel, D.; Toma, M.; Wysokińska, H.; Śliwiński, T. Anti-bacterial, anti-inflammatory, antioxidant, and antiproliferative properties of essential oils from hairy and normal roots of Leonurus sibiricus L. and their chemical composition. Oxid. Med. Cell. Longev., 2017, 2017, 7384061. PMID: 28191277
- Chandra, M.; Prakash, O.; Kumar, R.; Bachheti, R.K.; Bhushan, B.; Kumar, M.; Pant, A.K. β-Selinene-rich essential oils from the parts of Callicarpa macrophylla and their antioxidant and pharmacological activities. Medicines, 2017, 4(3), 52. doi: 10.3390/medicines4030052 PMID: 28930267
- Choo, G.S.; Lim, D.P.; Kim, S.M.; Yoo, E.S.; Kim, S.H.; Kim, C.H.; Woo, J.S.; Kim, H.J.; Jung, J.Y. Anti-inflammatory effects of Dendropanax morbifera in lipopolysaccharide stimulated RAW264.7 macrophages and in an animal model of atopic dermatitis. Mol. Med. Rep., 2019, 19(3), 2087-2096. PMID: 30747232
- Jeena, K.; Liju, V.B.; Kuttan, R. Antioxidant, anti-inflammatory and antinociceptive activities of essential oil from ginger. Indian J. Physiol. Pharmacol., 2013, 57(1), 51-62. PMID: 24020099
- Mahboubi, M. Zingiber officinale Rosc. essential oil, a review on its composition and bioactivity. Clinical Phytoscience, 2019, 5(1), 6. doi: 10.1186/s40816-018-0097-4
- Martins, F.T.; Doriguetto, A.C.; de Souza, T.C.; de Souza, K.R.D.; Dos Santos, M.H.; Moreira, M.E.C.; Barbosa, L.C.A. Composition, and anti-inflammatory and antioxidant activities of the volatile oil from the fruit peel of Garcinia brasiliensis. Chem. Biodivers., 2008, 5(2), 251-258. doi: 10.1002/cbdv.200890022 PMID: 18293438
- Queiroz, J.C.C.; Antoniolli, .R.; Quintans-Júnior, L.J.; Brito, R.G.; Barreto, R.S.; Costa, E.V.; da Silva, T.B.; Prata, A.P.N.; de Lucca, W., Jr; Almeida, J.R.; Lima, J.T.; Quintans, J.S. Evaluation of the anti-inflammatory and antinociceptive effects of the essential oil from leaves of Xylopia laevigata in experimental models. Sci. World J., 2014, 2014, 816450. PMID: 25097889
- Wan Salleh, W.M.N.H.; Kammil, M.F.; Ahmad, F.; Sirat, H.M. Antioxidant and anti-inflammatory activities of essential oil and extracts of Piper miniatum. Nat. Prod. commun., 2015, 10(11), 1934578-1501001151.
- da Silva, J.K.; da Trindade, R.; Moreira, E.C.; Maia, J.G.S.; Dosoky, N.S.; Miller, R.S.; Cseke, L.J.; Setzer, W.N. Chemical diversity, bio-logical activity, and genetic aspects of three Ocotea species from the Amazon. Int. J. Mol. Sci., 2017, 18(5), 1081. doi: 10.3390/ijms18051081 PMID: 28524091
- Han, X.; Beaumont, C.; Stevens, N. Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells. Biochim. Open, 2017, 5, 1-7. doi: 10.1016/j.biopen.2017.04.001 PMID: 29450150
- Purnima, B.M.; Kothiyal, P. A review article on phytochemistry and pharmacological profiles of Nardostachys jatamansi DC-medicinal herb. J. Pharmacogn. Phytochem., 2015, 3(5), 102-106.
- Marques, F.M.; Figueira, M.M.; Schmitt, E.F.P.; Kondratyuk, T.P.; Endringer, D.C.; Scherer, R.; Fronza, M. In vitro anti-inflammatory activity of terpenes via suppression of superoxide and nitric oxide generation and the NF-κB signalling pathway. Inflammopharmacology, 2019, 27(2), 281-289. doi: 10.1007/s10787-018-0483-z PMID: 29675712
- de Lavor, É.M.; Fernandes, A.W.C.; de Andrade Teles, R.B.; Leal, A.E.B.P.; de Oliveira Júnior, R.G.; Gama, E. Silva, M.; de Oliveira, A.P.; Silva, J.C.; de Moura Fontes Araújo, M.T.; Coutinho, H.D.M.; de Menezes, I.R.A.; Picot, L.; da Silva Almeida, J.R.G. Essential oils and their major compounds in the treatment of chronic inflammation: A review of antioxidant potential in preclinical studies and molecular mechanisms. Oxid. Med. Cell. Longev., 2018, 2018, 6468593. doi: 10.1155/2018/6468593 PMID: 30671173
- de Cássia da Silveira e Sá. R.; Andrade, L.N.; de Sousa, D.P. A review on anti-inflammatory activity of monoterpenes. Molecules, 2013, 18(1), 1227-1254. doi: 10.3390/molecules18011227 PMID: 23334570
- Huo, M.; Cui, X.; Xue, J.; Chi, G.; Gao, R.; Deng, X.; Guan, S.; Wei, J.; Soromou, L.W.; Feng, H. Anti-inflammatory effects of linalool in RAW 264.7 macrophages and lipopolysaccharide-induced lung injury model. J. Surg. Res., 2013, 180(1), e47-e54.
- Peana, A.T.; DAquila, P.S.; Panin, F.; Serra, G.; Pippia, P.; Moretti, M.D.L. Anti-inflammatory activity of linalool and linalyl acetate constituents of essential oils. Phytomedicine, 2002, 9(8), 721-726. doi: 10.1078/094471102321621322 PMID: 12587692
- Batista, P.A.; Werner, M.F.; Oliveira, E.C.; Burgos, L.; Pereira, P.; Brum, L.F.; Story, G.M.; Santos, A.R.S. The antinociceptive effect of (-)-linalool in models of chronic inflammatory and neuropathic hypersensitivity in mice. J. Pain, 2010, 11(11), 1222-1229. doi: 10.1016/j.jpain.2010.02.022 PMID: 20452289
- Valente, J.; Zuzarte, M.; Gonçalves, M.J.; Lopes, M.C.; Cavaleiro, C.; Salgueiro, L.; Cruz, M.T. Antifungal, antioxidant and anti-inflammatory activities of Oenanthe crocata L. essential oil. Food Chem. Toxicol., 2013, 62, 349-354. doi: 10.1016/j.fct.2013.08.083 PMID: 24012643
- Karimian, P.; Kavoosi, G.; Amirghofran, Z. Anti-oxidative and anti-inflammatory effects of Tagetes minuta essential oil in activated macrophages. Asian Pac. J. Trop. Biomed., 2014, 4(3), 219-227. doi: 10.1016/S2221-1691(14)60235-5 PMID: 25182441
- Kummer, R.; Fachini-Queiroz, F.C.; Estevão-Silva, C.F.; Grespan, R.; Silva, E.L.; Bersani-Amado, C.A.; Cuman, R.K.N. Evaluation of anti-inflammatory activity of Citrus latifolia Tanaka essential oil and limonene in experimental mouse models. Evid. Based Complement. Alternat. Med., 2013, 2013, 859083. PMID: 23762165
- Chi, G.; Wei, M.; Xie, X.; Soromou, L.W.; Liu, F.; Zhao, S. Suppression of MAPK and NF-κB pathways by limonene contributes to attenuation of lipopolysaccharide-induced inflammatory responses in acute lung injury. Inflammation, 2013, 36(2), 501-511. doi: 10.1007/s10753-012-9571-1 PMID: 23180366
- Bayala, B.; Bassole, I.H.N.; Gnoula, C.; Nebie, R.; Yonli, A.; Morel, L.; Figueredo, G.; Nikiema, J.B.; Lobaccaro, J.M.A.; Simpore, J. Chemical composition, antioxidant, anti-inflammatory and anti-proliferative activities of essential oils of plants from Burkina Faso. PLoS One, 2014, 9(3), e92122. doi: 10.1371/journal.pone.0092122 PMID: 24662935
- Salehi, B.; Upadhyay, S.; Erdogan Orhan, I.; Kumar Jugran, A.; L D Jayaweera, S.; A Dias, D.; Sharopov, F; Taheri,, Y.; Martins, N.; Baghalpour, N.; Cho, W.C.; Sharifi-Rad, J. Therapeutic potential of α- and β-Pinene: A miracle gift of nature. Biomolecules, 2019, 9(11), 738. doi: 10.3390/biom9110738 PMID: 31739596
- Bhoir, S.S.; Vishwapathi, V.; Singh, K.K. Antipsoriatic potential of Annona squamosa seed oil: An in vitro and in vivo evaluation. Phytomedicine, 2019, 54, 265-277. doi: 10.1016/j.phymed.2018.07.003 PMID: 30668377
- Muruganantham, N.; Basavaraj, K.H.; Dhanabal, S.P.; Praveen, T.K.; Shamasundar, N.M.; Rao, K.S. Screening of Caesalpinia bonduc leaves for antipsoriatic activity. J. Ethnopharmacol., 2011, 133(2), 897-901. doi: 10.1016/j.jep.2010.09.026 PMID: 20920562
- Singh, S.K.; Chouhan, H.S.; Sahu, A.N.; Narayan, G. Assessment of in vitro antipsoriatic activity of selected Indian medicinal plants. Pharm. Biol., 2015, 53(9), 1295-1301. doi: 10.3109/13880209.2014.976713 PMID: 25856701
- Saelee, C.; Thongrakard, V.; Tencomnao, T. Effects of Thai medicinal herb extracts with anti-psoriatic activity on the expression on NF-κB signaling biomarkers in HaCaT keratinocytes. Molecules, 2011, 16(5), 3908-3932. doi: 10.3390/molecules16053908 PMID: 21555979
- Vijayalakshmi, A.; Geetha, M. Anti-psoriatic activity of Givotia rottleriformis in rats. Indian J. Pharmacol., 2014, 46(4), 386-390. doi: 10.4103/0253-7613.135949 PMID: 25097275
- Müller, K.; Ziereis, K.; Gawlik, I. The antipsoriatic Mahonia aquifolium and its active constituents; II. Antiproliferative activity against cell growth of human keratinocytes. Planta Med., 1995, 61(1), 74-75. doi: 10.1055/s-2006-958005 PMID: 7700998
- Dhanabal, S.P.; Muruganantham, N.; Basavaraj, K.H.; Wadhwani, A.; Shamasundar, N.M. Antipsoriatic activity of extracts and fractions obtained from Memecylon malabaricum leaves. J. Pharm. Pharmacol., 2012, 64(10), 1501-1509. doi: 10.1111/j.2042-7158.2012.01528.x PMID: 22943181
- García-Pérez, M.E.; Allaeys, I.; Rusu, D.; Pouliot, R.; Janezic, T.S.; Poubelle, P.E. Picea mariana polyphenolic extract inhibits phlogogenic mediators produced by TNF-α-activated psoriatic keratinocytes: Impact on NF-κB pathway. J. Ethnopharmacol., 2014, 151(1), 265-278. doi: 10.1016/j.jep.2013.10.034 PMID: 24189030
- Vijayalakshmi, A.; Ravichandiran, V.; Velraj, M.; Nirmala, S.; Male, A.; Jayakumari, S.; Masilamani, K. Anti-Psoriatic activity of smilax china linn. rhizome. Indian J. Pharmaceut. Educat. Res., 2013, 47(1), 82-89.
- Dhanabal, S.P.; Priyanka Dwarampudi, L.; Muruganantham, N.; Vadivelan, R. Evaluation of the antipsoriatic activity of Aloe vera leaf extract using a mouse tail model of psoriasis. Phytother. Res., 2012, 26(4), 617-619. doi: 10.1002/ptr.3589 PMID: 21915932
- Parlapally, S.; Cherukupalli, N.; Bhumireddy, S.R.; Sripadi, P.; Anisetti, R.; Giri, C.C.; Khareedu, V.R.; Reddy Vudem, D. Chemical profil-ing and anti-psoriatic activity of methanolic extract of Andrographis nallamalayana J.L. Ellis. Nat. Prod. Res., 2016, 30(11), 1256-1261. doi: 10.1080/14786419.2015.1054825 PMID: 26153074
- Parmar, K.M.; Itankar, P.R.; Joshi, A.; Prasad, S.K. Anti-psoriatic potential of Solanum xanthocarpum stem in Imiquimod-induced psoriatic mice model. J. Ethnopharmacol., 2017, 198, 158-166. doi: 10.1016/j.jep.2016.12.046 PMID: 28052238
- Shrivastav, S.; Sindhu, R.; Kumar, S.; Kumar, P. Antipsoriatic and phytochemical evaluation of Thespesia populnea bark extracts. Int. J. Pharm. Pharm. Sci., 2009, 1(sup 1)
- Rajesh, B.; Albin, F.; Shilpesh, D.; Ramchandra, R.; Rajesh, S. Antipsoriatic effect of Tribulus terrestris extract by topical application in mouse model of contact dermatitis. Int. J. Vet. Sci., 2013, 2(1), 7-11.
- Dogra, N.K.; Kumar, S.; Thakur, K.; Kumar, D. Antipsoriatic effect of fatty acid enriched fraction of Vernonia anthelmintica Willd. fruits. J. Ethnopharmacol., 2018, 224, 85-90. doi: 10.1016/j.jep.2018.05.038 PMID: 29807119
- Gelmini, F.; Beretta, G.; Anselmi, C.; Centini, M.; Magni, P.; Ruscica, M.; Cavalchini, A.; Maffei Facino, R. GC-MS profiling of the phytochemical constituents of the oleoresin from Copaifera langsdorffii Desf. and a preliminary in vivo evaluation of its antipsoriatic effect. Int. J. Pharm., 2013, 440(2), 170-178. doi: 10.1016/j.ijpharm.2012.08.021 PMID: 22939967
- Sung, Y.Y.; Kim, H.K. Illicium verum extract suppresses IFN-γ-induced ICAM-1 expression via blockade of JAK/STAT pathway in Ha CaT human keratinocytes. J. Ethnopharmacol., 2013, 149(3), 626-632. doi: 10.1016/j.jep.2013.07.013 PMID: 23872327
- Li, K.; Zhou, R.; Wang Jia, W. Li, Z.; Li, J.; Zhang, P.; Xiao, T. Zanthoxylum bungeanum essential oil induces apoptosis of HaCaT human keratinocytes. J. Ethnopharmacol., 2016, 186, 351-361. doi: 10.1016/j.jep.2016.03.054 PMID: 27041402
Supplementary files
